Canonical Allele Identifier: CA819231241

Gene: TARID

Linked Data

• dbSNP Id: rs1159310603
• gnomAD v3: 6-133875550-G-C
• gnomAD v4: 6-133875550-G-C
• MyVariant Identifiers: chr6:g.134196688G>C (hg19) ; chr6:g.133875550G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875550G>C , CM000668.2:g.133875550G>C	GRCh38
NC_000006.11:g.134196688G>C , CM000668.1:g.134196688G>C	GRCh37
NC_000006.10:g.134238381G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.403+13054C>G